FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DERRICK SURESHIELD
K Number: K953712
·
Decision Oct 12, 1995
Classifications
1
FEI Numbers
138
Registration Numbers
138
Same Product Code
558
Applicant Total
2
Review Days
64
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Basic Information
- Device Name
- DERRICK SURESHIELD
- K Number
- K953712
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4460
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- M.P.S. Pharm'L Int'L
- Date Received
- August 9, 1995
- Decision Date
- October 12, 1995
- Product Code
- KGO
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KGO | Surgeon'S Gloves | FDA class 1 | General, Plastic Surgery |
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Other Clearances by M.P.S. Pharm'L Int'L
| K Number | Device Name | ||
|---|---|---|---|
| K953709 | DERRICK SAFETOUCH | Nov 6, 1995 | Substantially Equivalent |